rs1139807

This variant is located in the ACTG1 gene.

ClinVar annotation

Benign★★★
10 submitters5 publications

not specified; not provided; Autosomal dominant nonsyndromic hearing loss 20;Baraitser-winter syndrome 2; Baraitser-winter syndrome 2; Autosomal dominant nonsyndromic hearing loss 20

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About ACTG1

Actins are highly conserved proteins that are involved in various types of cell motility and in maintenance of the cytoskeleton. Three main groups of actin isoforms have been identified in vertebrate animals: alpha, beta, and gamma. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton and as mediators of internal cell motility. Actin gamma 1, encoded by this gene, is a cytoplasmic actin found in all cell types. Mutations in this gene are associated with DFNA20/26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss and also with Baraitser-Winter syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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